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Haploinsufficiency of Cyfip1 Produces Fragile X-Like Phenotypes in Mice
BACKGROUND: Copy number variation (CNV) at the 15q11.2 region, which includes a gene that codes for CYFIP1 (cytoplasmic FMR1 interacting protein 1), has been implicated in autism, intellectual disability and additional neuropsychiatric phenotypes. In the current study we studied the function of Cyfi...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3416859/ https://ncbi.nlm.nih.gov/pubmed/22900020 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0042422 |
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